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Amerisource Health Services

Amerisource Health Services Recalls

All product recalls associated with Amerisource Health Services.

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Recall Summary

Total Recalls

1000

Past Year

589

Class I (Serious)

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 6181–6200 of 10393 recalls

Dextroamphetamine Saccharate (Amerisource) – Mispackaging Risk (2016)

Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule

Class IIModerate

FDAAug 24, 2016Nationwide• Amerisource Health Services

Dextroamphetamine Saccharate (Amerisource) – Mispackaging Risk (2016)

Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule

Class IIModerate

FDAAug 24, 2016Nationwide• Amerisource Health Services

Dextroamphetamine Saccharate (Amerisource) – Mispackaging Risk (2016)

Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule

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Class II

Moderate

FDAAug 24, 2016Nationwide• Amerisource Health Services

Dextroamphetamine Saccharate (Amerisource) – Mispackaging Risk (2016)

Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule

Class IIModerate

FDAAug 24, 2016Nationwide• Amerisource Health Services

Dextroamphetamine Tablets (Amerisource) – Mispackaging Risk (2016)

Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule

Class IIModerate

FDAAug 24, 2016Nationwide• Amerisource Health Services

Dextroamphetamine Saccharate (Amerisource) – Mispackaging Risk (2016)

Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule

Class IIModerate

FDAAug 24, 2016Nationwide• Amerisource Health Services

Dextroamphetamine Saccharate (Amerisource) – Mispackaging Risk (2016)

Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule

Class IIModerate

FDAAug 24, 2016Nationwide• Amerisource Health Services

Dextroamphetamine Tablets (Amerisource) – Mispackaging Risk (2016)

Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule

Class IIModerate

FDAAug 24, 2016Nationwide• Amerisource Health Services

Dextroamphetamine Saccharate (Amerisource) – Mispackaging Risk (2016)

Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule

Class IIModerate

FDAAug 24, 2016Nationwide• Amerisource Health Services

Lamotrigine Tablets (Unichem) – Incorrect Tablet Imprint (2016)

Tablets/Capsules Imprinted With Wrong ID: incorrect imprint debossed on the tablets.

Class IIILow

FDAAug 19, 2016Nationwide• Unichem Pharmaceuticals Usa Inc

Football Helmets (Xenith) – head injury hazard (2016)

This recall involves Xenith Epic Varsity, X2 Varsity, X2E Varsity and Youth football helmets with a gloss or metallic-painted polycarbonate shell sold or factory-reconditioned between May 1, 2015 and March 18, 2016. The helmets were sold in multiple sizes depending on the model, and in varying colors and custom-paint designs. They have a facemask and a chin cup, available in different styles and varying colors, and may have an optional eye shield. The serial number is printed on a white sticker inside the top of the helmet. A complete list of the serial numbers included in this recall is available at www.xenith.com/recall.

CPSCAug 17, 2016Nationwide• Xenith LLC, of Detroit, Mich.

Rice Noodles (Louis Hong) – undeclared ingredients (2016)

Undeclared Allergen

Undeclared shrimp, soybean oil and green onions in fresh rice noodles.

Class IHigh

FDAAug 17, 2016IL• Louis Hong Inc Dba Mei Shun Noodle Inc

Kohler Portable Generators (Sumec) – Electrical Shock Risk (2016)

This recall involves the following Kohler portable generator models: PRO3.7, PRO3.7E, PRO5.2, PRO5.2E, and GEN5.0 with Spec Number PA-GEN50-3003. These generators have black frame assemblies and blue fuel tanks. The PRO3.7, PRO5.2 and GEN5.0 models have manual recoil start. The PRO3.7E and PRO5.2E have both manual recoil and electric start. Only generators with serial number 4528733735 or lower, and a manufacture date prior to 06 2016, representing the months and year of manufacture, are included in this recall. Model numbers, serial numbers, spec number and manufacturing date codes are on a silver label placed on each generator on the lower black frame assemblies.

CPSCAug 9, 2016Nationwide• Sumec Machinery & Electric Co. Ltd., of China

Cerovite Liquid (Pharmatech) – Bacterial Contamination (2016)

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Class IIModerate

FDAAug 8, 2016FL, MI, MS +1 more• Pharmatech LLC

Fer-Iron Liquid (Pharmatech) – Bacterial Contamination (2016)

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Class IIModerate

FDAAug 8, 2016FL, MI, MS +1 more• Pharmatech LLC

Tri-Vitamin (Pharmatech) – Bacterial Contamination (2016)

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Class IIModerate

FDAAug 8, 2016FL, MI, MS +1 more• Pharmatech LLC

Poly-Vita Drops with Iron (Pharmatech) – Bacterial Contamination (2016)

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Class IIModerate

FDAAug 8, 2016FL, MI, MS +1 more• Pharmatech LLC

Senna Syrup (Pharmatech) – Bacteria Contamination (2016)

CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.

Class IIModerate

FDAAug 8, 2016Nationwide• Pharmatech LLC

Polyvitamin Liquid (Pharmatech) – Bacterial Contamination (2016)

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Class IIModerate

FDAAug 8, 2016FL, MI, MS +1 more• Pharmatech LLC

Pedia Poly-Vite Drops (Pharmatech) – Contamination risk (2016)

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Class IIModerate

FDAAug 8, 2016FL, MI, MS +1 more• Pharmatech LLC